Under the quality policy of "Continuous improvement, high-quality products and higher customer satisfaction", the company constantly optimizes the quality management system and standardizes institutional regulations. We strictly implement domestic and international pharmaceutical quality standards as well as internal control specifications, and conduct production in full compliance with GMP requirements.Whole-process quality supervision and control are covered throughout supplier selection and evaluation, incoming raw material inspection, production process management, product testing and release, warehouse storage and product sales, so as to guarantee stable and reliable product quality. In September 2002, the company successfully passed the third-party ISO9001:2000 quality management system certification issued by SGS.
Meticulous evaluation of raw chemical precursors ensuring alignment with global purity benchmarks.
Continuous stoichiometric refinement and automated oversight across 24/7 industrial manufacturing operations.
Final molecular verification leveraging advanced analytical platforms to exceed specialized client specifications.
The Company’s Quality Inspection Department is currently equipped with professional analytical instruments, including:3 sets of High Performance Liquid Chromatograph (Waters e2695-2489) and 1 set of Ultra-High Performance Liquid Chromatograph (Waters UPLC-H-Class), mainly used for the determination of assay content and related substances of products;1 set of Gas Chromatograph (Agilent 6890N-7694E), dedicated to the detection of residual solvents;1 set of Atomic Absorption Spectrophotometer (PE-900H), applied to the analysis of heavy metals such as cadmium, cobalt, vanadium, nickel, lead, copper, antimony and lithium in finished products.